Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:122732425-122732776 | Common:2; Rare:107; Clinvar:2; Clinvar (benign):2 | ||||
chr4:122922897-122923163 | Common:2; Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr4:124712566-124713057 | Common:1; Rare:139 | ||||
chr4:127632698-127633010 | Common:2; Rare:70 | ||||
chr4:127880797-127880967 | Rare:57 | ||||
chr4:127965890-127966013 | Common:1; Rare:21; Clinvar (benign):2 | ||||
chr4:128061000-128061368 | Common:1; Rare:130 | ||||
chr4:129093494-129093753 | Rare:79 | ||||
chr4:133149070-133149346 | Common:2; Rare:80 | ||||
chr4:139177076-139177437 | Rare:94 | ||||
chr4:139301177-139301626 | Common:6; Rare:122 | ||||
chr4:139302445-139302477 | Rare:15 | ||||
chr4:139302480-139302506 | Rare:5 | ||||
chr4:139453652-139453825 | Common:2; Rare:59 | ||||
chr4:139453901-139454210 | Common:3; Rare:88; Clinvar:6; Clinvar (benign):4 |